The ability to provide sterile liquid products that meet corporate, scientific, regulatory, and end-user requirements can be a demanding task in today's environment. Through your implementation of ASEP-TECH® Blow/Fill/Seal technology, these application challenges can be met by the creative container and closure designs available with each system.
The scanners, sensors and terminals made available by PCE meet the most exacting of requirements for accuracy, reliability and speed of operation. The sensors are mechanically robust and extremely hardwearing.
The recovery of pharmaceutical active compounds requires special devices and features to protect the operator from contact. Nilfisk has designed a high containment filter unit (up to OEB5) for this application.
The Starweigh XS is a unique and highly precise checkweighing system delivering laboratory accuracies at high production throughput rates.
Complementing our commercial manufacturing and packaging services, we provide a range of commercial storage and distribution solutions for solid oral dosage forms and sterile biopharmaceuticals, for both niche / orphan drug products and large scale commercial market volumes.
Pilot Site Manager (PSM) is capable of supporting multiple line solutions forming the basis for unique item level serialization and aggregation of serial numbers to packaging units. The software manages the writing, reading, printing of serial numbers and the provision of serial numbers within the packaging environment. Pharmaceutical manufacturers can be assured of their compliance with legal requirements and brand protection demands while laying the foundation to meet future serialization regulations. All PCE systems are standards-based and 21 CFR Part 11 compliant.
HTR is the first fully automated rheometer available. Rheological measurements are carried out by MCR rheometers in the high quality the instruments are known for, while a robot handles all additional tasks pertaining to the measurement: sample loading, sample trimming and the cleaning of the upper and lower measuring system while the next measurement is already in progress.
The need to monitor headspace oxygen levels in parenteral containers arises from the requirement to ensure the stability and potency of oxygen-sensitive product.
In industrial biotech our know-how covers all process phases from upstream processing to cultivation and downstream purification with a variety of strategies for purification processes. We also have experience of bio-safety level 3 facilities.
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